Novel potent irriversible dual inhibitor of tubulin and epidermal growth factor receptor (EGFR), inducing the apoptosis of A549 cells in a dose- and time-dependent manner, along with decrease in mitochondrial membrane potential (MMP), production of ROS an

Novel inhibitor of β-catenin signaling, significantly reduced β-catenin activity in hepatoblastoma and several HCC cells

Potent anticancer tetrahydroisoquinoline alkaloid, being able to form a covalent bond with the amino group of a guanine in selected triplets of DNA duplexes and eventually give rise to double-strand breaks

Slightly less potent inhibitor of FMS than PLX647 but has better aqueous solubility

Novel polo-like kinase 1 (PLK1) inhibitor

Novel Inhibitor of the Polo-Box Domain of Polo-like Kinase 1 (Plk1 PBD)

Plk1 PBD-specific phosphopeptide inhibitor, effectively inhibiting mitotic progression and cell proliferation

Novel activator of AMPK, inducing apoptotic death in prostate cancer cells

Novel enhancer of Reactive Oxygen Species (ROS), depleting glutathione levels in analogy to piperlongumine but with reduced cell death

Novel inhibitor of phospholipase C (PLC) isozyme

Broad spectrum aminoglycoside antibiotic typically used for moderate-to-severe urinary tract infections or pyelonephritis

Gastroprotective agent, increasing the prostaglandin production in the gastric mucosa and accelerates ulcer healing

Novel Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2

Novel Potent and Specific Inhibitor of Placental Alkaline Phosphatase (PLAP; IC 50 = 32 nM), Targeting Tumor of the Female Reproductive Tract

Antilipidemic and antiplatelet agent

Potent inhibitor of HipA toxin, inhibiting E. coli persistence

Novel potent and specific β5i inhibitor

Novel highly potent and selective PKM2 inhibitor, blocking PKM2 mitochondrial translocation under nutritional stress and inhibits tumor growth in vivo

Novel selective inhibitor of protein kinase Cθ (PKCθ)

Novel Protein Kinase C-iota (PKC-ι) Inhibitor, Binding Post-kinase Domain Residues

Potent ligand to target the Y220C pocket, stabilizing Y220C

Inhibitor of topoisomerase II, intercalating into DNA and inducing topoisomerase II-mediated DNA strand crosslinks, resulting in inhibition of DNA replication and tumor cell cytotoxicity

Inhibitor of the acetylcholinesterase activity from bovine erythrocytes and electric eel

NSAID with better gastrointestinal (GI) tolerability

Natural nitric oxide (NO) production inhibitor

Novel potent in vitro and in vivo antifungal agent against azole-resistant Candida albicans

Antifungal antibiotic, showing inhibitory activity against fungi and yeasts, especially against Trichophyton

Antipsychotic prodrug, most notably used for schizophrenia

Inhibitor of PIP 4 Ks, efficiently killing transformed BJ cells, but not normal counterparts, displaying a strong selective lethality against Ras-activated or Ras-transformed cells

Antipsychotic agent